Clinical Trials Logo

Respiratory Failure clinical trials

View clinical trials related to Respiratory Failure.

Filter by:

NCT ID: NCT00297986 Completed - Healthy Clinical Trials

Evaluation of Different Interfaces for Noninvasive Positive Pressure Ventilation (NPPV)

Start date: June 2004
Phase: N/A
Study type: Observational

In this study the investigators aimed to study the ventilatory performance of different interfaces during NPPV delivering.

NCT ID: NCT00292097 Terminated - Clinical trials for Traumatic Brain Injury

A Prospective, Randomized Trial of Early Versus Late Tracheostomy in Trauma Patients With Severe Brain Injury

Start date: February 2006
Phase: N/A
Study type: Interventional

The purpose of this study is to evaluate the efficacy of early conversion tracheostomy from endotracheal intubation (ET) to percutaneous, dilatational tracheostomy (PDT) in traumatic brain-injured patients requiring prolonged mechanical ventilation.

NCT ID: NCT00291460 Recruiting - COPD Clinical Trials

Inspiratory Muscle Training in Hypercapnic COPD

Start date: February 2006
Phase: Phase 4
Study type: Interventional

The trial intends to investigate, whether inspiratory muscle training in hypercapnic patients improves inspiratory muscle strength, inspiratory muscle endurance and endurance to walk within six minutes.

NCT ID: NCT00282594 Completed - Sepsis Clinical Trials

The Effect of Intensive Insulin Therapy in the Surgical Critical Care Unit

Start date: July 2003
Phase: N/A
Study type: Interventional

We sought to determine if there is a benefit to using an insulin drip to control hyperglycemia in the surgical critical care unit for patients who undergo general and vascular surgery.

NCT ID: NCT00248729 Completed - Respiratory Failure Clinical Trials

Effectiveness and Safety Study of Etomidate Versus Midazolam to Help Place a Breathing Tube Outside of the Hospital.

Start date: October 2002
Phase: Phase 2
Study type: Interventional

The objective of this study was to compare the utility of etomidate and midazolam in helping patients to relax when there was a need for the placement of a ventilation tube by medics who were transporting patients to a hospital in an ambulance.

NCT ID: NCT00247468 Withdrawn - Sepsis Clinical Trials

Strict Glucose Control of Pediatric Intensive Care Unit (ICU) Patients

Start date: December 2004
Phase: N/A
Study type: Interventional

The study objective is to improve morbidity and mortality of high-risk critically ill children. Our hypothesis is that a strict ICU glucose control protocol will decrease morbidity and mortality associated with hyperglycemia in a population of high-risk critically ill pediatric patients.

NCT ID: NCT00221520 Active, not recruiting - Critical Illness Clinical Trials

Sedation in the Intensive Care Unit

Start date: February 2003
Phase: Phase 3
Study type: Interventional

High-risk critically ill patients often require mechanical ventilation either to primarily support the respiratory function or when the ventilation is insufficient to maintain adequate gas exchanges as a result of other organ impairment. In order to tolerate this aggressive mechanical support, enhance patient synchrony with the ventilator, and relieve pain and anxiety, analgesia and sedation are provided. It is suggested that an inappropriate use of sedation and analgesia may prolong the duration of mechanical ventilation and increase the risk of specific adverse outcomes such as ventilator associated pneumonia. Despite the widespread use of sedation, little information is available concerning the effect of varying the level of sedation on patients' subsequent mental health. We designed a randomized controlled trial to investigate the efficacy of sedation with the goal of maintaining the patient cooperative and interactive compared to the administration of sedation with the goal of maintaining the patient sedated. The first goal will be achieved by a discontinuous injection of a sedative, while the second goal will be achieved by a continuous infusion of the same sedative. In both groups pain relief will be provided in the same fashion with equal endpoints on a pain scoring scale. Our primary aim is to investigate whether differences in the occurrence of post-traumatic stress disorders (PTSD), anxiety, and depression are related to the choice of sedation-analgesia strategies. Secondary endpoints include the length of ICU stay, as indicated by the time to discharge from the ICU, the time to separation from mechanical ventilation, the rates of pulmonary and extra-pulmonary complications, and hospital length of stay. These endpoints will be compared between the two groups.

NCT ID: NCT00190346 Terminated - COPD Clinical Trials

Comparison of Humidification Devices During Non Invasive Ventilation, in Acute Respiratory Failure

Start date: December 2001
Phase: N/A
Study type: Interventional

Comparison of humidification devices during non invasive ventilation, in acute respiratory failure. The hypothesis was, due to dead space, lower humidification, a reduced efficiency of the technique (NIV) when HME are used in comparison with HH.

NCT ID: NCT00174070 Recruiting - Respiratory Failure Clinical Trials

Etiologies and Outcomes of Acute Respiratory Failure in Community

Start date: August 2005
Phase: N/A
Study type: Observational

Acute respiratory failure (ARF) remains a common reason for admission to the intensive care unit (ICU). ARF to be present in 32% of patients on ICU admission, with a further 24% of patients developing ARF during the ICU stay. A total of 56% of all ICU admissions for a length of >48 h had ARF at some point during their stay. The incidence of ARF was from 88.6 to 137.1 hospitalizations per 100,000 residents. The incidence of ARF was found to increase nearly exponentially with each decade until age 85 years. However, there is still paucity data about etiology and outcomes of acute respiratory failure happened in community. Mortality of ARF in critically ill patients is between 40% and 65%. Independent hazards for ARF mortality include older age, severe chronic co-morbidities (HIV, active malignancy, cirrhosis), certain precipitating events (trauma, drug overdose, bone marrow transplant), and multiple organ system failure (MOSF) [7-9]. Mortality has also been associated with acute lung injury or bilateral infiltrates on chest radiograph, and with an elevated acute physiology score. ARF patients form a large percentage of all ICU admissions and many factors might influence the final outcomes. With the high incidence of ARF in ICU, any improvement in the outcome of such population is likely to have marked effect on intensive care resource allocation. We wish this study may provide some valuable information about acute respiratory failure in community and improve the outcome of these patients.

NCT ID: NCT00148642 Completed - Respiratory Failure Clinical Trials

Silver-Coated Endotracheal Tube to Reduce Ventilator Associated Pneumonia (VAP)

NASCENT
Start date: November 2002
Phase: Phase 3
Study type: Interventional

The purpose of this study is to determine if the use of a silver-coated endotracheal tube (ETT) can reduce the incidence and/or delay the time of onset of VAP when compared to a non silver-coated ETT in patients who have been mechanically ventilated for >= 24 hours.